Vaccination Against Influenza H1N1 in Rheumatic Diseases
Primary Purpose
Influenza, Rheumatic Diseases
Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Focetria (Monovalent MF59-Adjuvanted vaccine)
Focetria (Monovalent MF59-Adjuvanted vaccine)
Focetria (Monovalent MF59-Adjuvanted vaccine)
Sponsored by
About this trial
This is an interventional prevention trial for Influenza focused on measuring rheumatoid, SLE, Psoriatic arthritis, Ankylosing, Influenza H1N1, Vaccine, Vaccination against H1N1 in rheumatic diseases
Eligibility Criteria
Inclusion Criteria:
- Patients suffering from: Rheumatoid Arthritis, Systemic Lupus Erythematosus, Ankylosing Spondylitis, Psoriatic Arthritis
- Able to firm an informed consent
- Aged - 18-65
- Candidates to receive vaccination against H1N1, according to the recommendation of the Ministry of Health
Exclusion Criteria:
- Allergy to eggs
- Known allergy to seasonal influenza vaccine
- Pregnant women
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Monovalent MF59-Adjuvanted vaccine
Arm Description
Outcomes
Primary Outcome Measures
Primary Endpoint : Proportion of patients who will achieve a titer of antibodies above 1/40 within the groups of patients in comparison with healthy subjects
Secondary Outcome Measures
Secondary Endpoint: Safety of the vaccine with regard to disease activity by changes in DAS, SLEDAI and BASDAI
Full Information
NCT ID
NCT01006681
First Posted
October 31, 2009
Last Updated
November 2, 2009
Sponsor
Tel-Aviv Sourasky Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT01006681
Brief Title
Vaccination Against Influenza H1N1 in Rheumatic Diseases
Official Title
Efficacy and Safety of Vaccination Against Influenza H1N1 in Patients With Rheumatoid Arthritis, Systemic Lupus Erythematosus, Psoriatic Arthritis and Ankylosing Spondylitis Treated With Immunomodulatory Drugs
Study Type
Interventional
2. Study Status
Record Verification Date
November 2009
Overall Recruitment Status
Unknown status
Study Start Date
November 2009 (undefined)
Primary Completion Date
April 2010 (Anticipated)
Study Completion Date
April 2010 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Tel-Aviv Sourasky Medical Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The spread of Influenza H1N1 has prompted the development of vaccines against this virus. Immunocompromised patients are at increased risk of developing complications of Influenza H1N1. The efficacy and safety of H1N1 vaccination have not been evaluated in this population of patients.
Detailed Description
100 patients with Rheumatoid Arthritis (RA), 50 patients with Systemic Lupus Erythematosus (SLE), 50 patients with spondyloarthropathies (Psoriatic arthritis (PsA) and Ankylosing Spondylitis (AS) and 200 healthy subjects will participate in the study.
All the subjects will be vaccinated with Focetria (Novartis) and will be evaluated the day of vaccination and 4 weeks later.
The evaluation will include:
Efficacy of the vaccine: Blood will be drawn on day 0 and 4 weeks later and tested for the presence of antibodies against A/California17/2009/H1N1 by hemagglutination inhibition test.
Safety of the vaccine:
Records of adverse event
Assessment of disease activity : RA - Disease activity score (DAS 28), SLE - SLEDAI, PsA - DAS 28 and PASI, AS- BASDAI, ESR, CRP
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Influenza, Rheumatic Diseases
Keywords
rheumatoid, SLE, Psoriatic arthritis, Ankylosing, Influenza H1N1, Vaccine, Vaccination against H1N1 in rheumatic diseases
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
400 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Monovalent MF59-Adjuvanted vaccine
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
Focetria (Monovalent MF59-Adjuvanted vaccine)
Other Intervention Name(s)
Focetria
Intervention Description
7.5 mcg Hemagglutinin H1/InfluezaA/California/7/2009 ,9.75 mg squalene MF59, 1.175 mg polysort80, 1.175 mg sorbitan trioleate
Intra muscular
Intervention Type
Biological
Intervention Name(s)
Focetria (Monovalent MF59-Adjuvanted vaccine)
Other Intervention Name(s)
Focetria
Intervention Description
7.5 mg Hemagglutinin H1/InfluezaA/California/7/2009, 9.75 mg squalene MF59, 1.175 mg polysirate 80, 1.175 mg sorbitan trioleate
Intramuscular injection
Intervention Type
Biological
Intervention Name(s)
Focetria (Monovalent MF59-Adjuvanted vaccine)
Other Intervention Name(s)
Focetria
Intervention Description
Monovalent MF59-Adjuvanted vaccine
Primary Outcome Measure Information:
Title
Primary Endpoint : Proportion of patients who will achieve a titer of antibodies above 1/40 within the groups of patients in comparison with healthy subjects
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Secondary Endpoint: Safety of the vaccine with regard to disease activity by changes in DAS, SLEDAI and BASDAI
Time Frame
4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients suffering from: Rheumatoid Arthritis, Systemic Lupus Erythematosus, Ankylosing Spondylitis, Psoriatic Arthritis
Able to firm an informed consent
Aged - 18-65
Candidates to receive vaccination against H1N1, according to the recommendation of the Ministry of Health
Exclusion Criteria:
Allergy to eggs
Known allergy to seasonal influenza vaccine
Pregnant women
12. IPD Sharing Statement
Citations:
PubMed Identifier
21425247
Citation
Elkayam O, Amir S, Mendelson E, Schwaber M, Grotto I, Wollman J, Arad U, Brill A, Paran D, Levartovsky D, Wigler I, Caspi D, Mandelboim M. Efficacy and safety of vaccination against pandemic 2009 influenza A (H1N1) virus among patients with rheumatic diseases. Arthritis Care Res (Hoboken). 2011 Jul;63(7):1062-7. doi: 10.1002/acr.20465.
Results Reference
derived
Learn more about this trial
Vaccination Against Influenza H1N1 in Rheumatic Diseases
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